Canonical Allele Identifier: CA823895840

Gene: APOM BAG6

Linked Data

• dbSNP Id: rs1156459296
• MyVariant Identifiers: chr6:g.31625305_31625307del (hg19) ; chr6:g.31657528_31657530del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31657530_31657532del , CM000668.2:g.31657530_31657532del	GRCh38
NC_000006.11:g.31625307_31625309del , CM000668.1:g.31625307_31625309del	GRCh37
NC_000006.10:g.31733286_31733288del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375916.4:c.442+52_442+54del (APOM) MANE Select	ENSP00000365081.3:n.442+52_442+54del
ENST00000375916.3:c.442+52_442+54del (APOM)	ENSP00000365081.3:n.442+52_442+54del
ENST00000375918.6:c.226+52_226+54del (APOM)	ENSP00000365083.2:n.226+52_226+54del
ENST00000375920.8:c.226+52_226+54del (APOM)	ENSP00000365085.4:n.226+52_226+54del
NM_001256169.1:c.226+52_226+54del (APOM)	NP_001243098.1:n.226+52_226+54del
NM_019101.2:c.442+52_442+54del (APOM)	NP_061974.2:n.442+52_442+54del
NR_045828.1:n.477+52_477+54del (APOM)
XM_006715150.2:c.346+52_346+54del (APOM)	XP_006715213.1:n.346+52_346+54del
XM_011514895.1:c.-14+2791_-14+2793del (BAG6)	XP_011513197.1:n.-14+2791_-14+2793del
XM_006715150.3:c.346+52_346+54del (APOM)	XP_006715213.1:n.346+52_346+54del
XM_017011279.2:c.-14+2791_-14+2793del (BAG6)	XP_016866768.1:n.-14+2791_-14+2793del
XM_024446545.1:c.-14+234_-14+236del (BAG6)	XP_024302313.1:n.-14+234_-14+236del
NM_019101.3:c.442+52_442+54del (APOM) MANE Select	NP_061974.2:n.442+52_442+54del
NM_001256169.2:c.226+52_226+54del (APOM)	NP_001243098.1:n.226+52_226+54del
NR_045828.2:n.483+52_483+54del (APOM)